HM13

An Error has occured retrieving Wikidata item for infobox HM13‏ (Histocompatibility minor 13) هوَ بروتين يُشَفر بواسطة جين HM13 في الإنسان.^[1]^[2]^[3]

الوظيفة

الأهمية السريرية

المراجع

^ "Entrez Gene: HM13 histocompatibility (minor) 13". مؤرشف من الأصل في 2010-12-05.
^ Weihofen A، Binns K، Lemberg MK، Ashman K، Martoglio B (يونيو 2002). "Identification of signal peptide peptidase, a presenilin-type aspartic protease". Science. ج. 296 ع. 5576: 2215–8. DOI:10.1126/science.1070925. PMID:12077416.
^ Nyborg AC، Kornilova AY، Jansen K، Ladd TB، Wolfe MS، Golde TE (أبريل 2004). "Signal peptide peptidase forms a homodimer that is labeled by an active site-directed gamma-secretase inhibitor". J Biol Chem. ج. 279 ع. 15: 15153–60. DOI:10.1074/jbc.M309305200. PMID:14704149.

قراءة متعمقة

Lemberg MK، Bland FA، Weihofen A، وآخرون (2002). "Intramembrane proteolysis of signal peptides: an essential step in the generation of HLA-E epitopes". J. Immunol. ج. 167 ع. 11: 6441–6. DOI:10.4049/jimmunol.167.11.6441. PMID:11714810.
Deloukas P، Matthews LH، Ashurst J، وآخرون (2002). "The DNA sequence and comparative analysis of human chromosome 20". Nature. ج. 414 ع. 6866: 865–71. DOI:10.1038/414865a. PMID:11780052.
Grigorenko AP، Moliaka YK، Korovaitseva GI، Rogaev EI (2002). "Novel class of polytopic proteins with domains associated with putative protease activity". Biochemistry Mosc. ج. 67 ع. 7: 826–35. DOI:10.1023/A:1016365227942. PMID:12139484.
McLauchlan J، Lemberg MK، Hope G، Martoglio B (2002). "Intramembrane proteolysis promotes trafficking of hepatitis C virus core protein to lipid droplets". EMBO J. ج. 21 ع. 15: 3980–8. DOI:10.1093/emboj/cdf414. PMC:126158. PMID:12145199.
Lemberg MK، Martoglio B (2002). "Requirements for signal peptide peptidase-catalyzed intramembrane proteolysis". Mol. Cell. ج. 10 ع. 4: 735–44. DOI:10.1016/S1097-2765(02)00655-X. PMID:12419218.
Strausberg RL، Feingold EA، Grouse LH، وآخرون (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. ج. 99 ع. 26: 16899–903. DOI:10.1073/pnas.242603899. PMC:139241. PMID:12477932.
Urny J، Hermans-Borgmeyer I، Gercken G، Schaller HC (2004). "Expression of the presenilin-like signal peptide peptidase (SPP) in mouse adult brain and during development". Gene Expr. Patterns. ج. 3 ع. 5: 685–91. DOI:10.1016/S1567-133X(03)00094-2. PMID:12972007.
Lehner B، Semple JI، Brown SE، وآخرون (2004). "Analysis of a high-throughput yeast two-hybrid system and its use to predict the function of intracellular proteins encoded within the human MHC class III region". Genomics. ج. 83 ع. 1: 153–67. DOI:10.1016/S0888-7543(03)00235-0. PMID:14667819.
Ota T، Suzuki Y، Nishikawa T، وآخرون (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs". Nat. Genet. ج. 36 ع. 1: 40–5. DOI:10.1038/ng1285. PMID:14702039.
Moliaka YK، Grigorenko A، Madera D، Rogaev EI (2004). "Impas 1 possesses endoproteolytic activity against multipass membrane protein substrate cleaving the presenilin 1 holoprotein". FEBS Lett. ج. 557 ع. 1–3: 185–92. DOI:10.1016/S0014-5793(03)01489-3. PMID:14741365.
Soares MR، Bisch PM، Campos de Carvalho AC، وآخرون (2004). "Correlation between conformation and antibody binding: NMR structure of cross-reactive peptides from T. cruzi, human and L. braziliensis". FEBS Lett. ج. 560 ع. 1–3: 134–40. DOI:10.1016/S0014-5793(04)00088-2. PMID:14988012.
Friedmann E، Lemberg MK، Weihofen A، وآخرون (2005). "Consensus analysis of signal peptide peptidase and homologous human aspartic proteases reveals opposite topology of catalytic domains compared with presenilins". J. Biol. Chem. ج. 279 ع. 49: 50790–8. DOI:10.1074/jbc.M407898200. PMID:15385547.
Gerhard DS، Wagner L، Feingold EA، وآخرون (2004). "The Status, Quality, and Expansion of the NIH Full-Length cDNA Project: The Mammalian Gene Collection (MGC)". Genome Res. ج. 14 ع. 10B: 2121–7. DOI:10.1101/gr.2596504. PMC:528928. PMID:15489334.
Otsuki T، Ota T، Nishikawa T، وآخرون (2007). "Signal sequence and keyword trap in silico for selection of full-length human cDNAs encoding secretion or membrane proteins from oligo-capped cDNA libraries". DNA Res. ج. 12 ع. 2: 117–26. DOI:10.1093/dnares/12.2.117. PMID:16303743.
Urny J، Hermans-Borgmeyer I، Schaller HC (2006). "Cell-surface expression of a new splice variant of the mouse signal peptide peptidase". Biochim. Biophys. Acta. ج. 1759 ع. 3–4: 159–65. DOI:10.1016/j.bbaexp.2006.02.007. PMID:16730383.
Loureiro J، Lilley BN، Spooner E، وآخرون (2006). "Signal peptide peptidase is required for dislocation from the endoplasmic reticulum". Nature. ج. 441 ع. 7095: 894–7. DOI:10.1038/nature04830. PMID:16738546.
Sato T، Nyborg AC، Iwata N، وآخرون (2006). "Signal peptide peptidase: biochemical properties and modulation by nonsteroidal antiinflammatory drugs". Biochemistry. ج. 45 ع. 28: 8649–56. DOI:10.1021/bi060597g. PMID:16834339.

هذه بذرة مقالة عن بروتين بحاجة للتوسيع. فضلًا شارك في تحريرها.

[entrez-1] "Entrez Gene: HM13 histocompatibility (minor) 13". مؤرشف من الأصل في 2010-12-05.

[pmid12077416-2] Weihofen A، Binns K، Lemberg MK، Ashman K، Martoglio B (يونيو 2002). "Identification of signal peptide peptidase, a presenilin-type aspartic protease". Science. ج. 296 ع. 5576: 2215–8. DOI:10.1126/science.1070925. PMID:12077416.

[pmid14704149-3] Nyborg AC، Kornilova AY، Jansen K، Ladd TB، Wolfe MS، Golde TE (أبريل 2004). "Signal peptide peptidase forms a homodimer that is labeled by an active site-directed gamma-secretase inhibitor". J Biol Chem. ج. 279 ع. 15: 15153–60. DOI:10.1074/jbc.M309305200. PMID:14704149.

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